Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

　　We are PCI.

　　Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

　　Summary of Objective:

　　The Validation Analyst I is responsible for overall validation project ownership of limited risk project(s) under heavy supervision. Responsible for the generation and execution of validation protocols, assistance in audits, and determination of validation needs. This job has no supervisory responsibilities.

　　Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned.

　　Performs validation activities to assure compliance to government and customer requirements.

　　Prepares validation protocols, validation statements, reports, summaries, and master validation plans for new customer/product/system project launches and maintains existing validated processes/programs at multiple sites as well as organizing and coordinating internal and customer approvals, as needed.

　　Ensures validation documentation completion, accuracy, and closure, including organizing and coordinating multiple approvals as required.

　　Prepares change control and validation history reports for audits.

　　Attends conference calls and meetings. Effectively communicates project goals and progress to Validation Supervisor / Manager.

　　Investigate validation deviations, document in formal reports, and ensure the resolution of corrective action to complete the project.

　　Primary contact for quality validation activities and managing expectations.

　　Reviews and interprets standards, procedures, and specifications for dissemination relative to validation protocols.

　　Knowledge of and adherence to all PCI, cGMP, GCP, GAMP, 21CFR, 21CFR Part 11, and Annex 11 policies, procedures, rules, and requirements.

　　Required to complete and pass a “Documentation Boot Camp” course within 6 months.

　　This position may require overtime and/or weekend work.

　　Attendance to work is an essential function of this position.

　　Performs other duties as assigned.

　　“Limited Risk Projects” are generally defined as projects/customer accounts that have the following.

　　Business needs of customers/projects require standard time commitments.

　　Low level of uncertainty in managing customer expectations.

　　Standard validation approach as documented in the Validation Plan.

　　Established criteria that are subject to minimal interpretation.

　　After basic training, this position will be required to specialize in 1 or more Validation areas of focus:Process/Cleaning ValidationsHVAC/Utility ValidationsComputer Validations

　　Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

　　Required:

　　High School Diploma or GED and/or 1-3 years related experience and/or training.

　　Basic Mathematical Skills

　　Basic Computer Skills: Ability to perform basic computer tasks and has the ability to operate common computer programs.

　　Minimum Professional Proficiency: Ability to speak in a way that allows one to participate effectively in various conversations. Ability to read various types of standard items addressed to general readers.

　　Intermediate Reasoning: Ability to apply common sense understanding to carry out instructions that may be furnished in written, oral, or diagram form. Ability to deal with problems that involve several concrete variables in standardized situations.

　　Preferred:

　　Process/Cleaning Validation Focus: Background in Packaging, Pharmaceutical, Bio-Pharmaceutical, and/or Medical Devices. Must be able to properly gown and work in an active packaging operation.

　　HVAC/Utility Validation Focus: Familiarity with HVAC wiring diagrams, control design, calibration, instrument configuration, and fundamentals of heating, air conditioning, and refrigeration systems.

　　Computer Validation Focus: Ability to perform complex computer tasks and have some experience with computer systems considered to have an impact on cGMP, cGXP, Annex 11, and PCI guidelines.

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　　Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future (https://pci.com/)

　　Equal Employment Opportunity (EEO) Statement:

　　PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

　　Why work for PCI Pharma Services?

　　At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don’t say no, we figure out how.

　　PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled